SNP Links for Protein (Select 53828710) - SNP

Links from Protein

Items: 1 to 20 of 392

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Select item 14906982161.

rs1490698216 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:55839353 (GRCh38)
11:55606829 (GRCh37)
Canonical SPDI:: NC_000011.10:55839352:T:C
Gene:: OR5D16 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.0002/1 (ALFA)
C=0.0002/1 (Estonian)
HGVS:: NC_000011.10:g.55839353T>C, NC_000011.9:g.55606829T>C, NM_001005496.1:c.602T>C, NP_001005496.1:p.Leu201Pro

Select item 14902978812.

rs1490297881 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 11:55838763 (GRCh38)
11:55606239 (GRCh37)
Canonical SPDI:: NC_000011.10:55838762:A:C,NC_000011.10:55838762:A:G
Gene:: OR5D16 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by cluster
MAF:: C=0.000004/1 (GnomAD_exomes)
G=0.000248/4 (TOMMO)
HGVS:: NC_000011.10:g.55838763A>C, NC_000011.10:g.55838763A>G, NC_000011.9:g.55606239A>C, NC_000011.9:g.55606239A>G, NM_001005496.1:c.12A>C, NM_001005496.1:c.12A>G

Select item 14884088083.

rs1488408808 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:55839340 (GRCh38)
11:55606816 (GRCh37)
Canonical SPDI:: NC_000011.10:55839339:A:G
Gene:: OR5D16 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.55839340A>G, NC_000011.9:g.55606816A>G, NM_001005496.1:c.589A>G, NP_001005496.1:p.Ser197Gly

Select item 14806912634.

rs1480691263 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:55838983 (GRCh38)
11:55606459 (GRCh37)
Canonical SPDI:: NC_000011.10:55838982:A:G
Gene:: OR5D16 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.55838983A>G, NC_000011.9:g.55606459A>G, NM_001005496.1:c.232A>G, NP_001005496.1:p.Ile78Val

Select item 14783559935.

rs1478355993 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:55839605 (GRCh38)
11:55607081 (GRCh37)
Canonical SPDI:: NC_000011.10:55839604:C:T
Gene:: OR5D16 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000011.10:g.55839605C>T, NC_000011.9:g.55607081C>T, NM_001005496.1:c.854C>T, NP_001005496.1:p.Pro285Leu

Select item 14721961556.

rs1472196155 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:55839539 (GRCh38)
11:55607015 (GRCh37)
Canonical SPDI:: NC_000011.10:55839538:T:C
Gene:: OR5D16 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000049/2 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.55839539T>C, NC_000011.9:g.55607015T>C, NM_001005496.1:c.788T>C, NP_001005496.1:p.Val263Ala

Select item 14718630577.

rs1471863057 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:55839230 (GRCh38)
11:55606706 (GRCh37)
Canonical SPDI:: NC_000011.10:55839229:C:A,NC_000011.10:55839229:C:T
Gene:: OR5D16 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000011.10:g.55839230C>A, NC_000011.10:g.55839230C>T, NC_000011.9:g.55606706C>A, NC_000011.9:g.55606706C>T, NM_001005496.1:c.479C>A, NM_001005496.1:c.479C>T, NP_001005496.1:p.Thr160Lys, NP_001005496.1:p.Thr160Ile

Select item 14668039738.

rs1466803973 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 11:55839520 (GRCh38)
11:55606996 (GRCh37)
Canonical SPDI:: NC_000011.10:55839519:A:C,NC_000011.10:55839519:A:G
Gene:: OR5D16 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.55839520A>C, NC_000011.10:g.55839520A>G, NC_000011.9:g.55606996A>C, NC_000011.9:g.55606996A>G, NM_001005496.1:c.769A>C, NM_001005496.1:c.769A>G, NP_001005496.1:p.Ile257Leu, NP_001005496.1:p.Ile257Val

Select item 14635356989.

rs1463535698 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:55839152 (GRCh38)
11:55606628 (GRCh37)
Canonical SPDI:: NC_000011.10:55839151:A:C
Gene:: OR5D16 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000011.10:g.55839152A>C, NC_000011.9:g.55606628A>C, NM_001005496.1:c.401A>C, NP_001005496.1:p.Tyr134Ser

Select item 145205700710.

rs1452057007 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:55839672 (GRCh38)
11:55607148 (GRCh37)
Canonical SPDI:: NC_000011.10:55839671:C:T
Gene:: OR5D16 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.55839672C>T, NC_000011.9:g.55607148C>T, NM_001005496.1:c.921C>T

Select item 145112153311.

rs1451121533 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:55839128 (GRCh38)
11:55606604 (GRCh37)
Canonical SPDI:: NC_000011.10:55839127:T:A
Gene:: OR5D16 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.55839128T>A, NC_000011.9:g.55606604T>A, NM_001005496.1:c.377T>A, NP_001005496.1:p.Val126Glu

Select item 144859480912.

rs1448594809 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:55839100 (GRCh38)
11:55606576 (GRCh37)
Canonical SPDI:: NC_000011.10:55839099:T:C
Gene:: OR5D16 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.55839100T>C, NC_000011.9:g.55606576T>C, NM_001005496.1:c.349T>C, NP_001005496.1:p.Phe117Leu

Select item 144825001113.

rs1448250011 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:55839626 (GRCh38)
11:55607102 (GRCh37)
Canonical SPDI:: NC_000011.10:55839625:A:G
Gene:: OR5D16 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000023/6 (TOPMED)
HGVS:: NC_000011.10:g.55839626A>G, NC_000011.9:g.55607102A>G, NM_001005496.1:c.875A>G, NP_001005496.1:p.Tyr292Cys

Select item 144595673114.

rs1445956731 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:55838827 (GRCh38)
11:55606303 (GRCh37)
Canonical SPDI:: NC_000011.10:55838826:C:A
Gene:: OR5D16 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.55838827C>A, NC_000011.9:g.55606303C>A, NM_001005496.1:c.76C>A, NP_001005496.1:p.Gln26Lys

Select item 144553771315.

rs1445537713 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 11:55839110 (GRCh38)
11:55606586 (GRCh37)
Canonical SPDI:: NC_000011.10:55839109:T:A,NC_000011.10:55839109:T:C
Gene:: OR5D16 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.55839110T>A, NC_000011.10:g.55839110T>C, NC_000011.9:g.55606586T>A, NC_000011.9:g.55606586T>C, NM_001005496.1:c.359T>A, NM_001005496.1:c.359T>C, NP_001005496.1:p.Met120Lys, NP_001005496.1:p.Met120Thr

Select item 144316298816.

rs1443162988 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:55839160 (GRCh38)
11:55606636 (GRCh37)
Canonical SPDI:: NC_000011.10:55839159:G:A
Gene:: OR5D16 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.55839160G>A, NC_000011.9:g.55606636G>A, NM_001005496.1:c.409G>A, NP_001005496.1:p.Ala137Thr

Select item 143587580517.

rs1435875805 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:55839403 (GRCh38)
11:55606879 (GRCh37)
Canonical SPDI:: NC_000011.10:55839402:A:C
Gene:: OR5D16 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000045/2 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
C=0.00002/5 (GnomAD_exomes)
HGVS:: NC_000011.10:g.55839403A>C, NC_000011.9:g.55606879A>C, NM_001005496.1:c.652A>C, NP_001005496.1:p.Thr218Pro

Select item 143455838518.

rs1434558385 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:55838995 (GRCh38)
11:55606471 (GRCh37)
Canonical SPDI:: NC_000011.10:55838994:A:G
Gene:: OR5D16 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000031/1 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.55838995A>G, NC_000011.9:g.55606471A>G, NM_001005496.1:c.244A>G, NP_001005496.1:p.Met82Val

Select item 143428136819.

rs1434281368 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:55839600 (GRCh38)
11:55607076 (GRCh37)
Canonical SPDI:: NC_000011.10:55839599:G:A
Gene:: OR5D16 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.55839600G>A, NC_000011.9:g.55607076G>A, NM_001005496.1:c.849G>A

Select item 143140961620.

rs1431409616 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:55839543 (GRCh38)
11:55607019 (GRCh37)
Canonical SPDI:: NC_000011.10:55839542:C:T
Gene:: OR5D16 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.55839543C>T, NC_000011.9:g.55607019C>T, NM_001005496.1:c.792C>T

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